Cas 145576-56-3,(1R,2R,3S)-2-Cyclohexylmethyl-3-(2-hydroxy-ethyl)-cyclopropanecarboxylic acid ((R)-1-phenyl-ethyl)-amide

145576-56-3

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Basic information

Product Name: (1R,2R,3S)-2-Cyclohexylmethyl-3-(2-hydroxy-ethyl)-cyclopropanecarboxylic acid ((R)-1-phenyl-ethyl)-amide
Synonyms:
CAS NO:145576-56-3
Molecular Formula:
Molecular Weight: 329.483
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1R,2R,3S)-2-Cyclohexylmethyl-3-(2-hydroxy-ethyl)-cyclopropanecarboxylic acid ((R)-1-phenyl-ethyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3S)-2-Cyclohexylmethyl-3-(2-hydroxy-ethyl)-cyclopropanecarboxylic acid ((R)-1-phenyl-ethyl)-amide(145576-56-3)
EPA Substance Registry System: (1R,2R,3S)-2-Cyclohexylmethyl-3-(2-hydroxy-ethyl)-cyclopropanecarboxylic acid ((R)-1-phenyl-ethyl)-amide(145576-56-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 145576-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145576-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,5,7 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145576-56:
(8*1)+(7*4)+(6*5)+(5*5)+(4*7)+(3*6)+(2*5)+(1*6)=153
153 % 10 = 3
So 145576-56-3 is a valid CAS Registry Number.

145576-56-3Upstream product

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145576-56-3Relevant academic research and scientific papers

Enantioselective, rhodium catalyzed intramolecular cyclopropanations of homoallylic diazoacetates

Martin, Stephen F.,Oalmann, Christopher J.,Liras, Spiros

, p. 6727 - 6730 (2007/10/02)

The homoallylic diazoacetates 3a-j underwent enantioselective intramolecular cyclopropanation with the rhodium catalyst Rh2(5S-MEPY)4 (1) to give the oxabicyclo[4.1.0]heptanes 4a-j in 71-90% enantiomeric excess and in 55-80% chemical

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